Regional Clinical Research Associate
Description/ Responsibilities
  • Study management, site management of study projects at local clinical sites
  • Responsible for monitoring of study activities
  • Coordinate all study activities to ensure protocol and regulatory requirement(s) are met (e.g. sample collection, sample processing, clinic set-up, etc.)
  • Adverse Event and Serious Adverse Event reporting
  • GCP compliant documentation for every project
  • Maintain adequate, accurate, complete and legible records.
  • Responsible for remaining current with regulatory requirements (DRAP, TPD, FDA, EMEA, UK MHRA etc.)
  • To perform any other duties as required, as training and experience allow.
  • Will perform tasks as assigned by supervisor.

M.B.B.S/ B.D.S, Registered Nurses, Medical Students,
M.Phil./ Ph.D., B. Pharm. / Pharm-D/
M. Pharm, B.Sc. (Biological Sciences), M.Sc. (Biological Sciences)

GCP Certification/ Clinical Research Certification Mandatory

Employment Type
Job Location
Rawalpindi/ Islamabad
Date posted
December 29, 2021
Valid through
January 10, 2022
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Position: Regional Clinical Research Associate

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